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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52294Erstellt: 24. Oktober 2026

4-Chlorobenzonitrile → 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide

https://huagongshe.com/de/reaction/52294

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorobenzonitrileHCID 12163—
Edukt4-(Methylsulfonyl)anilineHCID 79617—
EduktTrimethylaluminumHCID 16682925—
LösungsmittelTolueneHCID 1140—
LösungsmittelChloroformHCID 6212—
Produkt4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—

Reaktionsschritte

To a suspension of 4-(methylsulfonyl)aniline (7 g, 41 mmol) in toluene (400 mL), trimethylaluminum (2M solution in toluene, 30.5 mL, 61 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-chlorobenzonitrile (11.3 g, 82 mmol) in toluene (200 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 16 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (10.93 g, 86%) was used in the next reaction without further purification: mp (DSC) 191° C. Anal. Calc'd. for C14H13N2SO2Cl: C, 54.46, H, 4.24, N, 9.07. Found: C, 54.42, H, 4.30, N, 9.07.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616601
Quelldatensatzuspto-grants-1997_04
ORD IDord-45e2e30cff9d4228995f8b63eba08d26
Quellennotizuspto-grants-1997_04